Canonical Allele Identifier: CA1941478110
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508724T= , CM000672.2:g.122508724T= GRCh38
NC_000010.10:g.124268240T= , CM000672.1:g.124268240T= GRCh37
NC_000010.9:g.124258230T= NCBI36
NG_011554.1:g.52200T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1074T= MANE Select ENSP00000357980.3:p.Asp358=
ENST00000648167.1:c.756T= ENSP00000498033.1:p.Asp252=
ENST00000368984.7:c.1074T= ENSP00000357980.3:p.Asp358=
ENST00000420892.1:c.297T= ENSP00000412676.1:p.Asp99=
NM_002775.4:c.1074T= NP_002766.1:p.Asp358=
NM_002775.5:c.1074T= MANE Select NP_002766.1:p.Asp358=